Center of Molecular and Cellular Bioengineering, Biotechnology Center, Technische Universität Dresden, Dresden, Germany.
Department of Medicine, University of Cambridge, Cambridge, United Kingdom.
Elife. 2018 Jan 13;7:e29213. doi: 10.7554/eLife.29213.
Blood is arguably the most important bodily fluid and its analysis provides crucial health status information. A first routine measure to narrow down diagnosis in clinical practice is the differential blood count, determining the frequency of all major blood cells. What is lacking to advance initial blood diagnostics is an unbiased and quick functional assessment of blood that can narrow down the diagnosis and generate specific hypotheses. To address this need, we introduce the continuous, cell-by-cell morpho-rheological (MORE) analysis of diluted whole blood, without labeling, enrichment or separation, at rates of 1000 cells/sec. In a drop of blood we can identify all major blood cells and characterize their pathological changes in several disease conditions in vitro and in patient samples. This approach takes previous results of mechanical studies on specifically isolated blood cells to the level of application directly in blood and adds a functional dimension to conventional blood analysis.
血液可以说是最重要的体液,对其进行分析可以提供关键的健康状况信息。在临床实践中,缩小诊断范围的首要常规方法是进行差异血液计数,确定所有主要血细胞的频率。为了推进初始血液诊断,我们需要一种无偏且快速的血液功能评估方法,以便缩小诊断范围并生成具体的假设。为了满足这一需求,我们引入了连续的、逐个细胞的形态流变学(MORE)分析,无需标记、富集或分离,速度为 1000 个细胞/秒。在一滴血液中,我们可以识别所有主要的血细胞,并在体外和患者样本中对几种疾病条件下的细胞形态变化进行特征描述。这种方法将之前针对特定分离血细胞的机械研究结果提升到了直接在血液中应用的水平,并为传统的血液分析增加了一个功能维度。